NDC 66077-773 Instant Foam
NDC Product Code 66077-773
Proprietary Name: Instant Foam What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NDC Code Structure
- 66077 - Ultra-chem Inc.
- 66077-773 - Instant Foam
NDC 66077-773-25
Package Description: 199 g in 1 CAN
NDC 66077-773-26
Package Description: 454 g in 1 CAN
NDC Product Information
Instant Foam with NDC 66077-773 is a product labeled by Ultra-chem Inc.. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 616763.
Inactive Ingredient(s)
About the Inactive Ingredient(s)The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.
- PROPANE (UNII: T75W9911L6)
- BUTANE (UNII: 6LV4FOR43R)
- WATER (UNII: 059QF0KO0R)
Product Labeler Information
What is the Labeler Name?Name of Company corresponding to the labeler code segment of the Product NDC.
Labeler Name: Ultra-chem Inc.
Labeler Code: 66077
Start Marketing Date: 03-01-2010 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2017 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".
* Please review the disclaimer below.
Instant Foam Product Label Images
Instant Foam Product Labeling Information
The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.
Product Labeling Index
- Drug Facts Box Otc-Active Ingredients Section
- Drug Facts Box Otc-Purpose Section
- Drug Facts Box Otc-Indications And Usage Section
- Drug Facts Box Otc-Warnings Section
- Drug Facts Box Otc-When Using Section
- Drug Facts Box Otc-Stop Use Section
- Drug Facts Box Otc-Keep Out Of Reach Of Children Section
- Drug Facts Box Otc-Dosage & Administration Section
- Drug Facts Box Otc-Inactive Ingredients Section
- Instant Foam 4773 199G
Drug Facts Box Otc-Active Ingredients Section
Ethyl Alcohol 62%
Drug Facts Box Otc-Purpose Section
Antiseptic
Drug Facts Box Otc-Indications And Usage Section
For hand-washing to decrease bacteria on the skin, only when water is not available
Drug Facts Box Otc-Warnings Section
Flammable, keep away from fire and flamesFor external use only
Drug Facts Box Otc-When Using Section
Do not get into eyesif contact occurs, rinse eyes thoroughly with water
Drug Facts Box Otc-Stop Use Section
Irritation and redness develop
Drug Facts Box Otc-Keep Out Of Reach Of Children Section
If swallowed, get medical help or contact a Poison Control Center right away
Drug Facts Box Otc-Dosage & Administration Section
Press valve once to deliver one squirt (about a quarter size) of foaming product onto the palm of your handrub hands together and allow to dry without wiping
Drug Facts Box Otc-Inactive Ingredients Section
Water, DEA-C8-18 perfluoroalkylethyl phosphate, cetearyl alcohol, polysorbate 65, dimethicone PEG-8 meadowfoamate, meadowfoamamidopropyl betaine, butane, propane, fragrance
Instant Foam 4773 199G
477307F4150.jpg Instant Foam 199g
* Please review the disclaimer below.